Two Transient Receptor Potential Channels at Focal Adhesions

被引:2
作者
Mitsou, Ioli [1 ,4 ]
Carlson, Cathrine Rein [2 ,3 ]
Multhaupt, Hinke A. B. [1 ]
Brakebusch, Cord [1 ]
Couchman, John R. [1 ,5 ]
机构
[1] Univ Copenhagen, Biotech Res & Innovat Ctr, Copenhagen, Denmark
[2] Oslo Univ Hosp, Inst Expt Med Res, Oslo, Norway
[3] Univ Oslo, Oslo, Norway
[4] Agilent Technol Denmark ApS, Glostrup, Denmark
[5] Univ Copenhagen, Biotech Res & Innovat Ctr, Ole Maaloes Vej 5, DK-2200 Copenhagen N, Denmark
关键词
cell-matrix adhesion; cytoskeleton; epitope mapping; ion channel; junctions; INTEGRIN ADHESION; ION-CHANNEL; CELL-ADHESION; TRPM4; STRESS; MATRIX; FIBERS; FAK;
D O I
10.1369/00221554231194119
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Recently there have been reports that identify two transient receptor potential channels in cell-matrix junctions known as focal adhesions. These are the calcium channel TRP canonical 7 and the calcium-activated monovalent ion channel, TRP melastatin (TRPM) 4. Here, we report on the occurrence of TRPM4 in focal adhesions of fibroblasts. Of three commercial antibodies recognizing this channel, only one yielded focal adhesion staining, while the other two did not. The epitope recognized by the focal adhesion-localizing antibody was mapped to the extreme C-terminus of the TRPM4 protein. The other two antibodies bind to N-terminal regions of the TRPM4 proteins. Deletion of the TRPM4 gene by CRISPR/cas9 techniques confirmed that this channel is a bona fide focal adhesion component, while expression of full-length TRPM4 proteins suggested that processing may occur to yield a form that localizes to focal adhesions. Given the reports that this channel may influence migratory behavior of cells and is linked to cardiovascular disease, TRPM4 functions in adhesion should be explored in greater depth.
引用
收藏
页码:495 / 508
页数:14
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